125881 <common-name>4-[(2-Oxo-3,4-dihydro-1H-quinolin-7-yl)oxy]butanal</common-name> <description>4-[(2-Oxo-3,4-dihydro-1H-quinolin-7-yl)oxy]butanal is an organic compound with the chemical formula C13H15NO3 and an average molecular weight of 233.26 g/mol. 4-[(2-Oxo-3,4-dihydro-1H-quinolin-7-yl)oxy]butanal belongs to the quinolones and derivatives, a subclass of quinolines and derivatives within the organic compounds. The compound is associated with 13 recorded sources across multiple sectors. In the electrical and electronic equipment sector, it is found in cell phones, capacitors, batteries, printed circuit boards, wires and cables, and one additional source. Within textiles, leather and furnishings, it is present in carpets, rugs, and synthetic textiles. Other recorded sources include food packaging from the food, food processing and cookware sector, as well as medical devices from the healthcare, pharmaceuticals and veterinary products sector. Additionally, the compound is found in lubricants used in energy, oil and gas, as well as industrial manufacturing and chemical processing, along with one other sector. Recorded exposure routes for this compound include oral, inhalation, and touch.</description> <cas nil="true"/> <pubchem-id>56851120</pubchem-id> <chemical-formula>C13H15NO3</chemical-formula> <weight>233.26</weight> <appearance nil="true"/> <melting-point nil="true"/> <boiling-point nil="true"/> <density nil="true"/> <solubility nil="true"/> <specific-gravity nil="true"/> <flash-point nil="true"/> <vapour-pressure nil="true"/> <route-of-exposure nil="true"/> <target nil="true"/> <mechanism-of-toxicity nil="true"/> <metabolism nil="true"/> <toxicity nil="true"/> <lethaldose nil="true"/> <carcinogenicity nil="true"/> <use-source nil="true"/> <min-risk-level nil="true"/> <health-effects nil="true"/> <symptoms nil="true"/> <treatment nil="true"/> <created-at type="dateTime">2026-04-06T09:34:31Z</created-at> <updated-at type="dateTime">2026-08-28T00:17:56Z</updated-at> <interacting-proteins nil="true"/> <wikipedia nil="true"/> <uniprot-id nil="true"/> <kegg-compound-id nil="true"/> <omim-id nil="true"/> <chebi-id nil="true"/> <biocyc-id nil="true"/> <ctd-id nil="true"/> <stitch-id nil="true"/> <drugbank-id nil="true"/> <pdb-id nil="true"/> <actor-id nil="true"/> <organism nil="true"/> <export type="boolean">true</export> <metabolizing-proteins nil="true"/> <transporting-proteins nil="true"/> <moldb-smiles>C1CC(=O)NC2=C1C=CC(=C2)OCCCC=O</moldb-smiles> <moldb-formula>C13H15NO3</moldb-formula> <moldb-inchi>InChI=1S/C13H15NO3/c15-7-1-2-8-17-11-5-3-10-4-6-13(16)14-12(10)9-11/h3,5,7,9H,1-2,4,6,8H2,(H,14,16)</moldb-inchi> <moldb-inchikey>UEXWWBPDALYPLF-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">233.1051933</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>0.8</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id nil="true"/> <structure-image-file-name nil="true"/> <structure-image-content-type nil="true"/> <structure-image-file-size type="integer" nil="true"/> <structure-image-updated-at type="dateTime" nil="true"/> <biodb-id nil="true"/> <synthesis-reference nil="true"/> <structure-image-caption nil="true"/> <chemdb-id>CHEM121774</chemdb-id> <dsstox-id nil="true"/> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00116907</susdat-id> <iupac>4-[(2-oxo-3,4-dihydro-1H-quinolin-7-yl)oxy]butanal</iupac> <moldb-polar-surface-area nil="true"/> <moldb-refractivity nil="true"/> <moldb-polarizability nil="true"/> <moldb-rotatable-bond-count nil="true"/> <moldb-acceptor-count nil="true"/> <moldb-donor-count nil="true"/> <moldb-pka-strongest-acidic nil="true"/> <moldb-pka-strongest-basic nil="true"/> <moldb-physiological-charge nil="true"/> <moldb-number-of-rings nil="true"/> <moldb-alogps-logp nil="true"/> <moldb-alogps-logs nil="true"/> <moldb-alogps-solubility nil="true"/> <kingdom>Organic compounds</kingdom> <superklass>Organoheterocyclic compounds</superklass> <klass>Quinolines and derivatives</klass> <subklass>Quinolones and derivatives</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0159347</sync-id> <structure-inchikey>UEXWWBPDALYPLF-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>400000000000000008000000002000000000000000000000000000000000000000000000000202000000000000000000040000000000000000000800000000000000000000000008000000000000000200000000003000002000000000000000000000000000000000000201000000000000200000000000000080008000000200000080000000000002000000000000000000000000000000a00008000000000000000000000000000000800000000000000000800000000000400000000000000000100008000000000000200004000000000000000002002000000000000000000000000000000400000000100000000000000000a0004000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ������������������������€���`�������`�������(�������(�������h�������@(������@(������@h�������@h�������@(������@h��������(�������`�������`�������`�������h��������(��������������(��� �� ��h���h���h�� h� h� � ���� � ������������ �h�B�������������� ������������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:47:38Z</structure-indexed-at> </compound>